In Situ Photo-crosslinkable Hyaluronic Acid/Gelatin Hydrogel for Local Nitric Oxide Delivery

被引:4
作者
Catori, Daniele M. [1 ]
da Silva, Laura C. E. [1 ]
de Oliveira, Matheus F. [1 ]
Nguyen, Grace H. [2 ]
Moses, Joseph C. [2 ]
Brisbois, Elizabeth J. [2 ]
Handa, Hitesh [2 ,3 ]
de Oliveira, Marcelo G. [1 ]
机构
[1] Univ Campinas UNICAMP, Inst Chem, BR-13083970 Campinas, Brazil
[2] Univ Georgia, Coll Engn, Sch Chem Mat & Biomed Engn, Athens, GA 30602 USA
[3] Univ Georgia, Coll Pharm, Pharmaceut & Biomed Sci Dept, Athens, GA 30602 USA
基金
巴西圣保罗研究基金会; 美国国家卫生研究院;
关键词
hyaluronic acid; gelatin; nitric oxide; hydrogels; in situ cross-linking; tissue regeneration; EXTRACELLULAR-MATRIX; POLY(VINYL ALCOHOL); CELL-PROLIFERATION; ACID; SCAFFOLDS; RELEASE; PLGA;
D O I
10.1021/acsami.3c10030
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
An increasing number of studies have shown that the local release of nitric oxide (NO) from hydrogels stimulates tissue regeneration by modulating cell proliferation, angiogenesis, and inflammation. The potential biomedical uses of NO-releasing hydrogels can be expanded by enabling their application in a fluid state, followed by controlled gelation triggered by an external factor. In this study, we engineered a hydrogel composed of methacrylated hyaluronic acid (HAGMA) and thiolated gelatin (GELSH) with the capacity for in situ photo-cross-linking, coupled with localized NO release. To ensure a gradual and sustained NO release, we charged the hydrogels with poly-(l-lactic-co-glycolic acid) (PLGA) nanoparticles functionalized with S-nitrosoglutathione (GSNO), safeguarding SNO group integrity during photo-cross-linking. The formation of thiol-ene bonds via the reaction between GELSH's thiol groups and HAGMA's vinyl groups substantially accelerated gelation (by a factor of 6) and increased the elastic modulus of hydrated hydrogels (by 1.9-2.4 times). HAGMA/GELSH hydrogels consistently released NO over a 14 day duration, with the release of NO depending on the hydrogels' equilibrium swelling degree, determined by the GELSH-to-HAGMA ratio. Biocompatibility assessments confirmed the suitability of these hydrogels for biological applications as they display low cytotoxicity and stimulated fibroblast adhesion and proliferation. In conclusion, in situ photo-cross-linkable HAGMA/GELSH hydrogels, loaded with PLGA-GSNO nanoparticles, present a promising avenue for achieving localized and sustained NO delivery in tissue regeneration applications.
引用
收藏
页码:48930 / 48944
页数:15
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